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For example, some studies find that LepA is ubiquitous [ 13- 15] but this finding has not been confirmed by others [ 16].
Other reports have linked CMV disease to steroid use, but this finding has not yet been confirmed [26 28].
A single migraine study using a candidate-gene approach was performed in 2010 identifying a rare mutation in the TRESK potassium channel segregating in a large family with migraine with aura, but this finding has later become questioned.
One study has reported reduced levels of LRP in the brains of AD patients [19], but this finding has not been confirmed by others [20].
Previous studies have revealed an association between a common genetic variant in NOS1AP and QT interval in populations of European ancestry, but this finding has not been extended to other ethnic populations.
Several studies have suggested an association between periodontal disease and prematurity but this finding has not been consistently observed.
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82– 84 A single pathological study carried out in 4 dystoniatonia brains found perinuclear inclusion bodies in midbrain reticular formation and periaqueductal gray matter, 85 but so far this finding has not been replicated, with the remainder of pathological studies not having detected any specific abnormalities.
These preliminary results are promising but the clinical significance of this finding has to be determined in larger studies.
Antibodies to gangliosides and Purkinje cells have been reported in celiac patients with neuropathy and ataxia [ 148, 149], but the pathogenic role of this finding has not been clearly demonstrated [ 150, 151].
In addition, most Somali women had obvious problems with weak upper leg muscles, but this finding had no statistically significant association with low 25(OH D levels.
This finding has generated huge controversy.
More suggestions(16)
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Justyna Jupowicz-Kozak
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